US4883657A - Rearranger process and composition for permanent waving process - Google Patents
Rearranger process and composition for permanent waving process Download PDFInfo
- Publication number
- US4883657A US4883657A US07/158,209 US15820988A US4883657A US 4883657 A US4883657 A US 4883657A US 15820988 A US15820988 A US 15820988A US 4883657 A US4883657 A US 4883657A
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- US
- United States
- Prior art keywords
- hair
- composition
- rearranging
- thioglycolate
- salt
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/737—Galactomannans, e.g. guar; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8158—Homopolymers or copolymers of amides or imides, e.g. (meth) acrylamide; Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/04—Preparations for permanent waving or straightening the hair
Definitions
- This invention relates broadly to a hair waving or curling process and a novel rearranging waving lotion composition for use in a waving or curling process.
- keratin a proteinaceous material
- the hair's keratin is made up of long fibrous polypeptide chains which are bonded together with horizontal cross bonds of two forms: Hydrogen bonds and cystine bonds, also sometimes referred to as disulfide bonds.
- Cystine bonds play an essential role in determining the degree of curl in hair. Some researchers in the field believe that straight or slightly wavy hair has relatively fewer cystine bonds and relies heavily upon hydrogen bonding to produce curl or waves in the hair and that very curly hair has a relatively larger amount of cystine bonds. Other researchers in the field believe that straight hair and curly hair may have the same number of cystine bonds, but that the cystine bonds present in straight hair tend to occur in a relatively straight alignment, whereas the cystine bonds present in curly hair tend to occur out of alignment.
- Permanent hair waving is usually carried out by subjecting the hair to a strong reducing agent, such as hydroxide or, more commonly, materials containing a free "--SH” group or thiol. These "thiol” materials are also called mercaptans. In this treatment, the hair is saturated with the thiol agent, which then acts to break the disulfide bonds.
- the hair is rinsed, removing the unreacted thiol waving agent and disulfide reaction product.
- the hair is then realigned, e.g., usually by winding on rollers, in order to physically align previously unpaired hair protein bonds, i.e., one-half of the cystine groups.
- the hair and rollers are then saturated with an oxidizing agent, or neutralizer, such as hydrogen peroxide or a bromate salt, to reform disulfide bonds between the newly paired hair protein thiols and to give the hair a configuration of wave.
- This general process may be used to either add curl or straighten the hair.
- Salts of thioglycolic acid such as ammonium thioglycolate, and thioglycolic acid esters, such as glycerol thioglycolate, are typically utilized as the thiol waving agent.
- Other thiol-containing reagents such as thiolactic acid, betamercaptopropionic acid, beta-mercaptobutyric acid, mercaptosuccinic acid and alike have been suggested in the art to be effective.
- Another problem that occurs during the hair disulfide bond breaking process is skin irritation caused by the thiol-containing agents. Irritation occurs usually because beauticians frequently use their bare fingers for the wrapping process.
- an object of the present invention is to provide an improved hair waving process and further to provide an improved rearranger composition for use in a hair waving process.
- the present invention is a process of waving hair by applying to the hair a particular rearranging composition with chemical properties sufficient to change the alignment of the cystine bonds in the hair keratin.
- the rearranging composition comprises a homogenous mixture of a salt of thioglycolic acid and a cationic homopolymer of methylacrylamidopropyltrimethyl ammonium chloride.
- a wrapping lotion composition is then applied to the hair.
- the hair, with wrapping lotion applied is wrapped around a rod or roller to produce a desired curl pattern.
- the hair with wrapping lotion applied is left on the rods for a predetermined length of time, preferably about 5 to about 15 minutes, in order to set or lock in the desired curl pattern.
- the wrapped hair is rinsed to flush away excess wrapping lotion composition.
- a neutralizer composition is applied to the hair, still on the rods, to lock in the curl pattern.
- the neutralizer is left on the hair for a sufficient period of time to reestablish the cystine bonds, after which the neutralizer is flushed away by rinsing the hair.
- the improved rearranger comprises a salt of thioglycolatic acid and between about 1.00 and about 3.0% by weight of a cationic homopolymer of methacrylamidopropyltrimethyl ammonium chloride.
- the rearranger also includes between about 6.0 and about 10.0% by weight of ammonium thioglycolate, between about 3.0 and about 7.0% by weight of monoethanolamine thioglycolate.
- the rearranger has a pH of between about 8.0 and about 10.5.
- the waving process of the instant invention is comprised of several steps, some of which involve the application of specific hair treatment formulations.
- a rearranging composition is applied to the hair to perform a straightening function.
- the rearranging composition contains an aqueous solution of chemical agents capable of reducing the disulfide linkages in hair keratin.
- Suitable chemical agents include water soluable mercaptans, e.g. salts of thioglycolic acid, such as sodium, monoethanolamine, or ammonium thioglycolate, and magnesium thioglycolate.
- Other soluble mercaptans include thioglycerol, sodium or potassium borohydride, and sodium or ammonium sulfite.
- the amount of these chemical agents may vary depending on, among other things, the degree of straightening desired, hair treatment history, and the chemical nature of the particular hair to be treated.
- a preferred rearranging composition comprises a mixture of ammonium thioglycolate and monoethanolamine thioglycolate ("MEA-Thio").
- MEA-Thio monoethanolamine thioglycolate
- the ammonium thioglycolate is preferably present inconcentration ranges of about 6.0 to about 10.0% by weight of the rearranging composition
- the MEA-Thio is preferably present in concentrations of about 3.0 to about 7.0% by weight of the total composition.
- the ammonium thioglycolate and MEA-Thio together preferably comprise between about 7.0% and about 16.0% by weight of the total rearranger composition.
- a most preferred rearranging composition comprises about 8.0% by weight of ammonium thioglycolate and about 5.5% by weight MEA-Thio.
- the rearranging composition may be characterized by the weight ratio of ammonium thioglycolate to MEA-Thio.
- a preferred ratio is between about 4:6 about 7:3 ammonium thioglycolate to MEA-Thio, with a most preferred ratio of 6:4.
- the preferred concentration is between about 5.0 and about 20% by weight.
- a variety of conventional additives may be present in the rearranging composition, such as, conditioners perfumes, emollients, etc.
- the pH of the composition is adjusted to between 8.0 and 10.5, preferably using ammonium hydroxide.
- a polyquaternary amine salt is a highly charge cationic homopolymer of methacrylamidopropyltrimethyl ammonium chloride (MAPTAC).
- a preferred concentration of MAPTAC is from between about 1.0 to about 3.0% by weight of the rearranging composition, with a most preferred concentration of about 2.0% by weight.
- the average molecular weight of the MAPTAC homopolymer ranges from about 100,000 to about 200,000.
- the MAPTAC increases the longevity of the curl pattern and the humectant qualities of the hair by penetrating the hair.
- the neutralizer solution When the neutralizer solution is applied the polymer is believed to become “locked” into the hair.
- the increased integrity of the hair and the curl pattern that results from the application of MAPTAC greatly reduces the need for maintenance between subsequent waving treatments.
- a variety of conventional additives may be present in the rearranging composition, such as, conditioners, perfumes, moisturizers, emollients, etc.
- the pH of the composition is adjusted to between 8.0 and 10.5 using, preferably, ammonium hydroxide.
- the rearranging composition is initially applied to the head and worked into the hair with gentle combing.
- the rearranging composition is allowed to stand, on the hair for about 5-15 or 20 minutes while the cystine bonds are being broken, the length of time the rearranger is allowed to stand depends upon the degree of curl in the hair's natural state and the degree of straightness desired.
- the hair is rinsed, preferably with warm water for about 3-5 minutes to flush away the major portion, preferably all, of the rearranging composition. In this way, the rearranging composition and the wrapping lotion composition are not applied to the hair at the same time.
- a wrapping lotion or booster is applied to the head and gently massaged into the hair.
- the hair is then wrapped on rods, curlers, rollers or any other means known to the art to produce or establish a desired curl pattern.
- the wrapped hair containing the wrapping lotion is allowed to stand for a period of about 5-15 minutes, while the pattern of the curl becomes set.
- the wrapped hair is then rinsed with warm water to remove any excess of wrapping lotion composition.
- neutralizer After rinsing, a neutralizer is applied to the wrapped hair to restore the disulfide linkages in the hair keratin.
- the neutralizer "locks in” the curl pattern that was formed in the previous steps of the waving process.
- the exact composition of the neutralizer is not believed critical to achieve the improved results obtained by the waving process of the invention.
- neutralizers are typically aqueous solutions containing oxidizing agents, such as, sodium bromate. Other ingredients may be added to the neutralizer composition to improve the aesthetic properties of the hair. In particular, it has been found that the addition of from about 1.0 to about 5.0% by weight of ethoxylated castor oil greatly improves the sheen quality of the hair.
- sealer may be applied to the hair to alleviate the initial dryness that sometimes results immediately after the hair has undergone a waving process.
- sealers contain conditioners and humectants.
- a rearranging composition was prepared for use and evaluation in a waving process.
- a first solution was prepared by combining and mixing deionized water and a cationic homopolymer of MAPTAC. This solution was then heated to about 80° C.
- a second soultion of surfactants, conditioners and moisturizers was prepared and heated to about 80° C. The second solution was combined with the first solution and mixed for about 20 minutes and the resultant admixture was allowed to cool to about 50° C.
- a third solution of monoethanolamine thioglycolate, fragrance and a pH adjuster was then added to the admixture and mixed slowly until a homogenous solution was obtained.
- the relative weight fractions of the components in the composition are listed in Table II.
- a waving process in accordance with the invention was performed using the rearranging composition of Example I.
- the first step in the process involved preshampooing the head with a suitable conditioning shampoo.
- the hair was then towel blotted dry.
- the rearranging composition of Example I was then applied to the hair by a tint-brush procedure in an effect to minimize scalp irritation.
- the rearranger used comprised a homogenous mixture of MEA thioglycolate and a homopolymer of MAPTAC. The rearranger was allowed to stand on the hair for about 10 to 15 minutes until straight.
- the hair was rinsed thoroughly for about 3 to 5 minutes with warm water, then towel blotted dry.
- a wrapping lotion was then applied in 1/4 head sections. The hair in each 1/4 section was then wrapped on rods to produce a curl pattern. After roding, the wrapping lotion was allowed to stand on the hair for about 10 minutes.
- the hair with the rods intact was then rinsed thoroughly with warm water and then towel blotted dry.
- a conventional neutralizer solution having sodium bromate as the active ingredient was then applied sparingly to each rodded portion of hair and allowed to stand for about 10 minutes under a plastic wrap. After processing with the neutralizer, the rodded hair was then rinsed well with warm water for about 3 to 5 minutes to substantially remove the neutralizer. The hair was then unrodded, rinsed again, and dried under a conventional hair dryer.
- the resultant hair style obtained from the waving process of the instant invention was characterized as being thicker, more full bodied than hair styles previously possible using prior art waving process.
- the longevity of the curl pattern produced and humectant qualities of the hair was increased on a relatively long term bases with substantially lower need for application of maintenance products.
- the improved hair characteristics obtained as a result of the instant process is believe directly attributable to the use of the improved rearranging composition containing the homopolymer of MAPTAC.
- Example III For the purposes of comparison to the improved waving process of the invention as described in Example III, a conventional prior art waving process was performed.
- the procedure used for the conventional waving process was identical to that of the waving process of Example III with the exception that the rearranger used did not contain a homopolymer of MAPTAC.
- the rearranger used was the formulation described above in Example II.
- the resultant hair style obtained from the conventional waving process was characterized as relatively tightly curled, dry, and frizzy in appearance. Furthermore, this style required the application of maintenance products, such as, moisturizers and curl activators. These maintenance caused an overall greasy look of the hair style.
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- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Abstract
Description
TABLE I ______________________________________ Formulation A Formulation B ______________________________________ Deionized H.sub.2 O 59.7 59.6 MAPTAC 2.0 -- Ammonium Thioglycolate 8.0 10.0 MEA Thioglycolate 5.5 -- Other Ingredients.sup.1 24.8 30.4 ______________________________________ .sup.1 Conditioners, surfactants, pH adjusters, moisturizers and fragrance.
Claims (13)
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/158,209 US4883657A (en) | 1988-02-19 | 1988-02-19 | Rearranger process and composition for permanent waving process |
BR898905998A BR8905998A (en) | 1988-02-19 | 1989-02-14 | PROCESS FOR HAIR CURLING |
PCT/US1989/000689 WO1989007435A2 (en) | 1988-02-19 | 1989-02-14 | Permanent wave process and compositions |
EP19890903397 EP0356508A4 (en) | 1988-02-19 | 1989-02-14 | Permanent wave process and compositions |
OA59528A OA09233A (en) | 1988-02-19 | 1989-02-17 | Permanent waving process and compositions. |
CA000591386A CA1323816C (en) | 1988-02-19 | 1989-02-17 | Permanent waving process and compositions |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/158,209 US4883657A (en) | 1988-02-19 | 1988-02-19 | Rearranger process and composition for permanent waving process |
Publications (2)
Publication Number | Publication Date |
---|---|
US4883657A true US4883657A (en) | 1989-11-28 |
US4883657B1 US4883657B1 (en) | 1992-05-12 |
Family
ID=22567107
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US07/158,209 Expired - Fee Related US4883657A (en) | 1988-02-19 | 1988-02-19 | Rearranger process and composition for permanent waving process |
Country Status (1)
Country | Link |
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US (1) | US4883657A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5476650A (en) * | 1994-03-17 | 1995-12-19 | Luster Products, Inc. | Conditioning and straightening hair relaxer |
US5863526A (en) * | 1997-01-10 | 1999-01-26 | Rhone-Poulenc, Inc. | Homopolymers prepared from ammonium quaternary salts of aminoalkylacrylamides |
US6058943A (en) * | 1999-07-18 | 2000-05-09 | Davis-Harris; Pamela | Formulation and method for smoothing and waving multi-textured hair |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4391286A (en) * | 1981-02-19 | 1983-07-05 | Helene Curtis Industries | Hair conditioning and composition therefor |
US4416297A (en) * | 1980-01-23 | 1983-11-22 | Clairol Incorporated | Hair waving or straightening process and product |
US4572220A (en) * | 1981-02-19 | 1986-02-25 | Helene Curtis Industries, Inc. | Composition for altering the configuration of hair |
US4588760A (en) * | 1985-08-09 | 1986-05-13 | Clairol Incorporated | Hair treatment composition |
US4602648A (en) * | 1984-10-30 | 1986-07-29 | Soft Sheen Products, Inc. | Pre-shampoo normalizer for a hair straightening system |
-
1988
- 1988-02-19 US US07/158,209 patent/US4883657A/en not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4416297A (en) * | 1980-01-23 | 1983-11-22 | Clairol Incorporated | Hair waving or straightening process and product |
US4391286A (en) * | 1981-02-19 | 1983-07-05 | Helene Curtis Industries | Hair conditioning and composition therefor |
US4572220A (en) * | 1981-02-19 | 1986-02-25 | Helene Curtis Industries, Inc. | Composition for altering the configuration of hair |
US4602648A (en) * | 1984-10-30 | 1986-07-29 | Soft Sheen Products, Inc. | Pre-shampoo normalizer for a hair straightening system |
US4588760A (en) * | 1985-08-09 | 1986-05-13 | Clairol Incorporated | Hair treatment composition |
Non-Patent Citations (5)
Title |
---|
"Guar Gum and Its Application", by R. J. Chudzikowski, Soc. Cosmet. Chem. 22, 43-60 (1971), Society of Cosmetic Chemist of Great Britian. |
A Product Brochure from High Tek Polymers Inc. * |
A Product Brochure from High-Tek Polymers Inc. |
Celanese Corporation Product Bulletins Nos. 114, 38, 23, 122, CN 175, CN 176, CN 174, 117, 118, 123, 124, 180. * |
Guar Gum and Its Application , by R. J. Chudzikowski, Soc. Cosmet. Chem. 22, 43 60 (1971), Society of Cosmetic Chemist of Great Britian. * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5476650A (en) * | 1994-03-17 | 1995-12-19 | Luster Products, Inc. | Conditioning and straightening hair relaxer |
US5863526A (en) * | 1997-01-10 | 1999-01-26 | Rhone-Poulenc, Inc. | Homopolymers prepared from ammonium quaternary salts of aminoalkylacrylamides |
US6058943A (en) * | 1999-07-18 | 2000-05-09 | Davis-Harris; Pamela | Formulation and method for smoothing and waving multi-textured hair |
GB2363329B (en) * | 1999-07-18 | 2004-03-24 | Pamela Harris | Formulation and method for smoothing and waving multi-textured hair |
Also Published As
Publication number | Publication date |
---|---|
US4883657B1 (en) | 1992-05-12 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: SOFT SHEEN PRODUCTS, INC., A DE CORP. Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNORS:WILLIAMS, BARRY W.;DANIELS, PAMELA M.;REEL/FRAME:004860/0570 Effective date: 19880219 Owner name: SOFT SHEEN PRODUCTS, INC.,ILLINOIS Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:WILLIAMS, BARRY W.;DANIELS, PAMELA M.;REEL/FRAME:004860/0570 Effective date: 19880219 |
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Owner name: CONTINENTAL BANK N.A. Free format text: SECURITY INTEREST;ASSIGNOR:AMETHYST INVESTMENT GROUP, INC.;REEL/FRAME:005221/0051 Effective date: 19890228 |
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Owner name: AMETHYST INVESTMENT GROUP, INC. Free format text: CHANGE OF NAME;ASSIGNOR:SOFT SHEEN PRODUCTS INC.;REEL/FRAME:005203/0076 Effective date: 19890101 |
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Owner name: FIRST NATIONAL BANK OF CHICAGO, THE Free format text: SECURITY INTEREST;ASSIGNOR:AMETHYST INVESTMENT GROUP, INC., (F/K/A SOFT SHEEN PRODUCTS, INC.);REEL/FRAME:005437/0777 Effective date: 19900823 |
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RR | Request for reexamination filed |
Effective date: 19901120 |
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B1 | Reexamination certificate first reexamination | ||
REMI | Maintenance fee reminder mailed | ||
LAPS | Lapse for failure to pay maintenance fees | ||
FP | Lapsed due to failure to pay maintenance fee |
Effective date: 19891128 |
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STCH | Information on status: patent discontinuation |
Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362 |